Dimerization and direct membrane interaction of Nup53 contribute to nuclear pore complex assembly

EMBO Journal

Volumn 31, Issue 20, 2012, Pages 4072-4084

  Vollmer, Benjamin ^a   Schooley, Allana ^a   Sachdev, Ruchika ^a   Eisenhardt, Nathalie ^a   Schneider, Anna M ^b   Sieverding, Cornelia ^a   Madlung, Johannes ^c   Gerken, Uwe ^d   MacEk, Boris ^c   Antonin, Wolfram ^a  

^a FRIEDRICH MIESCHER LABORATORY OF THE MAX PLANCK SOCIETY   (Germany)

^b MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d UNIVERSITY OF HOHENHEIM   (Germany)

Author keywords

nuclear envelope formation; nuclear membrane; nuclear pore complex assembly; Nup35; Nup53

Indexed keywords

MEMBRANE PROTEIN; NUCLEOPORIN; NUP53 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CELL FUNCTION; CELL NUCLEUS MEMBRANE; CELL PROLIFERATION; CONTROLLED STUDY; DIMERIZATION; IN VITRO STUDY; INTERPHASE; MITOSIS; NONHUMAN; NUCLEAR PORE COMPLEX; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; VERTEBRATE; YEAST;

AMINO ACID SEQUENCE; ANIMALS; BINDING SITES; CONSERVED SEQUENCE; DIMERIZATION; HELA CELLS; HUMANS; INTERPHASE; LIPOSOMES; MEMBRANE FUSION; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; NUCLEAR PORE; NUCLEAR PORE COMPLEX PROTEINS; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; SACCHAROMYCES CEREVISIAE PROTEINS; STRUCTURE-ACTIVITY RELATIONSHIP; XENOPUS LAEVIS; XENOPUS PROTEINS;

VERTEBRATA;

EID: 84867572986     PISSN: 02614189     EISSN: 14602075     Source Type: Journal    
DOI: 10.1038/emboj.2012.256     Document Type: Article

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